A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230875



Internal ID20797915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79533787..80226538hg38UCSC Ensembl
chr10:81293543..81986294hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38692752
hg19692752
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586915
Supporting Variants
Samples
Known GenesANXA11, BEND3P3, LINC00857, LOC100288974, LOC642361, MBL1P, NUTM2B, PLAC9, SFTPA1, SFTPA2, SFTPD, TMEM254, TMEM254-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230875
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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